A representative intensity map (CD18) is shown in Figure 2, A and B. The density of the grayscale pattern was proportional to the signal intensity of a peptide peak at a certain m/z, retention time, and charge state.
A clear tendency of increased exosome quantity was seen by fluorescence intensity (Figure 3B, n = 5). Figure 3C is a Western blot of one representative experiment for the exosomal marker CD63 reflecting the higher protein amount under stressed conditions.
At steady state (24 hr after induction) for each dose, single gene transcription sites were captured at 15 min intervals for ∼ 15 hr, resulting in representative transcription intensity traces shown in Figure 2E,F (red, green lines, Video 4).
Representative figures are shown in Figure 1A.
The representative fluorescence intensity profiles are shown in Figure 4b.
Figure 4 shows representative fluorescence intensity decays of Me-ADOTA·Cl measured on SWs (blue line) and on empty areas (red line).
Representative maximum intensity projections of confocal image stacks from each of the three probe combinations (18 & 19, 7 & 18 and 7 & 19) are shown in Figure 2, panels A C, respectively.
Figure 3 (the upper panel) demonstrates representative maximum intensity projection (MIP) PET images of nude mice bearing NCI-H2122 tumor xenografts, scanned on days 0, 1, and 3 after the treatment with vehicle (Figure 3a) and RO4987655, 5.0 mg/kg (Figure 3c).
The representative IHC intensity of c-Met expression is described in Figure 2.
A representative maximum intensity projection of this tracking is shown in Figure 2A with the two data sets shown in different colors.
A representative figure showing the correlation between log2 signal intensities is presented in Figure 1A which shows r = 0.98, suggesting acceptable reproducibility.
